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European Journal of Prosthodontics and Restorative Dentistry  —  Vol. 34, Issue Special Issue 7 (August 2026) ← Back to issue
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Disappearing Umbilical Cord, Disrupted Body Wall: Late Sonographic Diagnosis of Body Stalk Anomaly—A Case Report and Literature Review

DOI: 10.1922/ejprd.v34i7s.1636
Keywords

Body stalk anomaly; limb-body wall complex; abdominal wall defect; prenatal ultrasound; fetal anomaly; case report

Authors

1Yohana Natalia N, Department of Obstetrics
and Gynaecology, Faculty of Medicine,
Universitas Airlangga, Surabaya, Indonesia

2Nareswari Imanadha Cininta M
Department of Obstetrics and Gynaecology,
Faculty of Medicine, Universitas Airlangga,
Surabaya, Indonesia, Department of Obstetrics
and Gynaecology, Dr. Soetomo Academic
General Hospital, Surabaya, Indonesia

3Manggala Pasca Wardhana
Department of Obstetrics and Gynaecology,
Faculty of Medicine, Universitas Airlangga,
Surabaya, Indonesia, Department of Obstetrics
and Gynaecology, Dr. Soetomo Academic
General Hospital, Surabaya, Indonesia

Received:14-06-2026
Revised: 20-07-2026
Accepted: 28-07-2026

European Journal of Prosthodontics and Restorative Dentistry (2026) 34(7s), 433–438

Disappearing Umbilical Cord, Disrupted Body Wall: Late Sonographic Diagnosis of Body Stalk Anomaly—A Case Report and Literature Review

Abstract

Background: Body stalk anomaly (BSA), also known as limb-body wall complex (LBWC), is an extremely rare and almost uniformly lethal disruption of early embryonic folding. Because of its lethality, the central clinical challenge lies in early identification and accurate diagnosis, which are essential for appropriate antenatal counselling and management. Case Presentation: We report a 27-week gestation in a 2nd-gravida woman referred for a suspected fetal abdominal wall defect detected on antenatal ultrasound. Sonography demonstrated a large ventral wall defect with herniation of abdominal contents, ventriculomegaly, kyphoscoliosis, and an abnormally short umbilical cord with direct placental attachment, consistent with body stalk anomaly. Because the condition was incompatible with extrauterine survival, the pregnancy was terminated. The male neonate, born vaginally, weighed 1000 g with an Apgar score of 1/0 and showed a giant closed omphalocele, spina bifida, anorectal malformation, low-set ears, and bilateral congenital talipes equinovarus (CTEV); the herniated viscera remained covered by amniotic membrane and were directly continuous with the placenta. Conclusion: Body stalk anomaly must be distinguished early from other, more survivable, anterior abdominal wall defects such as gastroschisis and omphalocele, because its prognosis and counselling implications differ substantially. First-trimester ultrasound remains the cornerstone of diagnosis, enabling timely, informed decision-making for affected families.

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Article Information
Pages
433 – 438
Cover Date
August 2026
Volume
34
Issue
Special Issue 7
Print ISSN
0965-7452
Electronic ISSN
2396-8893